Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2082520 | Drug Discovery Today: Technologies | 2013 | 8 Pages |
Abstract
Allosteric modulators (AMs) are a promising avenue towards safe and selective drugs. AMs can interact selectively with unique domains distinct from the endogenous ligand binding site of receptors, up- or down-regulating the response to receptor activation. Emphasis is placed in this article on the latest development in high-sensitivity technologies designed to identify AMs of G-protein coupled receptors. In addition to new pharmacological approaches, encouraging results in the crystal resolution of these targets enable use of more rational approaches to identification and optimization of AMs.
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Authors
Robert Lütjens, Benjamin Perry, Dominik Schelshorn, Jean-Philippe Rocher,